Metabolic Features of Multiple Myeloma

被引:61
作者
El Arfani, Chaima [1 ]
De Veirman, Kim [1 ]
Maes, Ken [1 ]
De Bruyne, Elke [1 ]
Menu, Eline [1 ]
机构
[1] Vrije Univ Brussel, Myeloma Ctr Brussels, Dept Hematol & Immunol, B-1090 Brussels, Belgium
关键词
metabolism; multiple myeloma; bone marrow micro-environment; BONE-MARROW MICROENVIRONMENT; DRUG-RESISTANCE; CANCER-CELLS; GLUCOSE-METABOLISM; TUMOR-CELLS; GLUTAMINE-METABOLISM; THERAPEUTIC TARGET; LACTATE; 2-DEOXY-D-GLUCOSE; ANGIOGENESIS;
D O I
10.3390/ijms19041200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer is known for its cellular changes contributing to tumour growth and cell proliferation. As part of these changes, metabolic rearrangements are identified in several cancers, including multiple myeloma (MM), which is a condition whereby malignant plasma cells accumulate in the bone marrow (BM). These metabolic changes consist of generation, inhibition and accumulation of metabolites and metabolic shifts in MM cells. Changes in the BM micro-environment could be the reason for such adjustments. Enhancement of glycolysis and glutaminolysis is found in MM cells compared to healthy cells. Metabolites and enzymes can be upregulated or downregulated and play a crucial role in drug resistance. Therefore, this review will focus on changes in glucose and glutamine metabolism linked with the emergence of drug resistance. Moreover, metabolites do not only affect other metabolic components to benefit cancer development; they also interfere with transcription factors involved in proliferation and apoptotic regulation.
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页数:19
相关论文
共 127 条
[1]   Ammonium Production and Glutamine-Addiction of Myeloma Cells: New Attractive Targets in Multiple Myeloma [J].
Accardi, Fabrizio ;
Chiu, Martina ;
Bolzoni, Marina ;
Storti, Paola ;
Todoerti, Katia ;
Agnelli, Luca ;
Ferrari, Massimiliano ;
Missale, Gabriele ;
Aversa, Franco ;
Bussolati, Ovidio ;
Giuliani, Nicola .
BLOOD, 2014, 124 (21)
[2]  
Alfarouk Khalid O, 2014, Oncoscience, V1, P777
[3]  
Alfarouk Khalid O, 2011, Cancers (Basel), V3, P3002, DOI 10.3390/cancers3033002
[4]   From Krebs to clinic: glutamine metabolism to cancer therapy [J].
Altman, Brian J. ;
Stine, Zachary E. ;
Dang, Chi V. .
NATURE REVIEWS CANCER, 2016, 16 (10) :619-634
[5]   The cytotoxicity of 3-bromopyruvate in breast cancer cells depends on extracellular pH [J].
Azevedo-Silva, Joao ;
Queiros, Odilia ;
Ribeiro, Ana ;
Baltazar, Fatima ;
Young, Ko H. ;
Pedersen, Peter L. ;
Preto, Ana ;
Casal, Margarida .
BIOCHEMICAL JOURNAL, 2015, 467 :247-258
[6]   Targeting glutamine metabolism in multiple myeloma enhances BIM binding to BCL-2 eliciting synthetic lethality to venetoclax [J].
Bajpai, R. ;
Matulis, S. M. ;
Wei, C. ;
Nooka, A. K. ;
Von Hollen, H. E. ;
Lonial, S. ;
Boise, L. H. ;
Shanmugam, M. .
ONCOGENE, 2016, 35 (30) :3955-3964
[7]   Dysfunctional T cell metabolism in the tumor microenvironment [J].
Beckermann, Kathryn E. ;
Dudzinski, Stephanie O. ;
Rathmell, Jeffrey C. .
CYTOKINE & GROWTH FACTOR REVIEWS, 2017, 35 :7-14
[8]   Promising therapies in multiple myeloma [J].
Bianchi, Giada ;
Richardson, Paul G. ;
Anderson, Kenneth C. .
BLOOD, 2015, 126 (03) :300-310
[9]   Dependence on glutamine uptake and glutamine addiction characterize myeloma cells: a new attractive target [J].
Bolzoni, Marina ;
Chiu, Martina ;
Accardi, Fabrizio ;
Vescovini, Rosanna ;
Airoldi, Irma ;
Storti, Paola ;
Todoerti, Katia ;
Agnelli, Luca ;
Missale, Gabriele ;
Andreoli, Roberta ;
Bianchi, Massimiliano G. ;
Allegri, Manfredi ;
Barilli, Amelia ;
Nicolini, Francesco ;
Cavalli, Albertina ;
Costa, Federica ;
Marchica, Valentina ;
Toscani, Denise ;
Mancini, Cristina ;
Martella, Eugenia ;
Dall'Asta, Valeria ;
Donofrio, Gaetano ;
Aversa, Franco ;
Bussolati, Ovidio ;
Giuliani, Nicola .
BLOOD, 2016, 128 (05) :667-679
[10]   Glucose transporters: Structure, function and consequences of deficiency [J].
Brown, GK .
JOURNAL OF INHERITED METABOLIC DISEASE, 2000, 23 (03) :237-246